Archive
577 recalls were announced in August 2022.
Of the 577 recalls this month scored against our rubric, 1% are Critical, 15% are Severe.
Which agencies issued them
Mckesson Medical-Surgical is recalling Fisher Scientific Sure-Vue RPR Dispensing Pipettes due to temperature excursions during storage from June to August 2021. Exposure to higher temperatures may have impacted product effectiveness.
BD Vacutainer blood collection tubes are recalled due to potential temperature damage during storage from June to August 2021. Affected tubes received between June 1 and September 30, 2021 may have reduced effectiveness.
Mckesson is recalling Dynarex DynaLube lubricating jelly due to facility temperature excursions from June-August 2021 that may have degraded product effectiveness. Recall affects 17.5 boxes distributed nationwide between June-September 2021.
Mckesson Medical-Surgical initiated a voluntary nationwide recall of Fisherbrand SWAB TRANS STUARTS swabs. The specific reason for the recall is not documented in the FDA notice.
Materialise USA LLC is recalling ProPlan CMF Anatomical Model units where packages labeled MU22-INA-DUQ contained the wrong anatomical model inside. Recipients should verify their package contents match the label.
Mckesson Medical-Surgical Inc. is recalling Dynarex Nail Polish Remover Pads due to facility temperature excursions in summer 2021 that may have reduced product effectiveness. All lots received between June 1 and September 30, 2021, nationwide are affected.
Mckesson Medical-Surgical is recalling Medline catheter insertion trays (Model DYND10160) due to temperature excursions at the manufacturing facility that may have affected product effectiveness. Affected units were distributed nationwide between June and September 2021.
Dynarex lemon glycerin swabs distributed nationwide may have reduced effectiveness due to temperature excursions prior to delivery. All lots received between June 1 and September 30, 2021 are affected.
Oshkosh is recalling certain Shepphard steering gears for S-Series 2.0 vehicles because incorrect assembly may cause the gear to fracture, potentially leading to a loss of steering control.
Connoisseur’s Kitchen is recalling approximately 880 pounds of imported frozen ready-to-eat chicken entrees due to possible Listeria monocytogenes contamination. No illnesses have been reported.
REV is recalling 2018-2023 motorhome models from Fleetwood and Holiday Rambler because hydraulic lines may be improperly routed or protected, risking fluid leaks that could cause fires. Dealers will repair free of charge.
Porsche is recalling 2001-2020 models because missing caps on headlight adjustment screws can cause improper alignment, increasing crash risk.
Wayfarer is recalling 2017-2020 Tiffin Wayfarer motorhomes because wheel lug nuts may not have been properly tightened during a previous repair, posing a crash risk.
Roadtrek is recalling certain 2022 Zion, Zion SRT, Chase, and Zion Slumber motorhomes because front seat mounting bolts may be improperly tightened, potentially failing to restrain occupants during a crash.
Daimler Trucks North America is recalling certain 2020-2023 Western Star 47X and 49X commercial trucks because hood bezel covers may detach, creating a road hazard and increasing crash risk. Approximately 3,498 vehicles are affected.
DRV is recalling 2021-2022 Mobile Suites fifth wheels because tail, stop, and turn lights may be placed too high, reducing visibility and increasing crash risk.
Kia is recalling certain 2023 Sportage vehicles because the alternator battery positive terminal nut may loosen, risking engine stall or fire. Dealers will inspect and tighten the terminal nut free of charge.
Cruise LLC is recalling Automated Driving System units with specific software versions that may incorrectly predict vehicle paths during unprotected left turns, increasing crash risk.
Volkswagen Group of America is recalling 2022 Audi A3, S3, and RS3 vehicles because the front passenger air bag may be folded incorrectly, increasing injury risk in a crash.
Dennis Eagle is recalling 2021-2022 Proview Dual Steer vehicles because a steering cross shaft may separate, causing loss of steering control and increasing crash risk.
Ford is recalling 2022 Mustang Mach-E vehicles because the right-rear axle half shafts may break under load, potentially causing loss of drive power or a rollaway.
Ford is recalling 2015-2017 Expedition and Navigator vehicles because a failing front blower motor may increase the risk of an interior fire.
Forest River is recalling 2023 Flagstaff and Rockwood fifth wheels because the Federal Placard lists an incorrect axle rating (5,200 lbs instead of 5,000 lbs), which could lead to vehicle overloading and increased crash risk.
Chrysler is recalling certain 2022 RAM 2500, 3500, 4500, and 5500 vehicles with Cummins diesel engines. The engine control module may have a misaligned capacitor that can short-circuit, causing loss of drive power and increasing crash risk.
Ford is recalling 2017-2020 F-Super Duty and Lincoln Continental vehicles because a degrading camera lens coating can cause a foggy rearview image, increasing crash risk.
Hino is recalling 2023 NJ7A and NV7A trucks because an engine control module defect may cause unexpected engine shutdown, increasing crash risk.
Agit Global stand-up paddleboard paddles can suddenly break mid-shaft during use, exposing sharp edges. About 124,000 units sold nationwide from 2015–2020 pose a risk of serious puncture or laceration injuries.
General Motors is recalling 2013-2015 Chevrolet Spark and 2014-2015 Spark EV vehicles because the secondary hood latch may corrode, preventing proper engagement and increasing crash risk.
PT. Elangperdana Tyre Industry is recalling specific Zeetex AT 1000 tires because the sidewall may separate, increasing crash risk.
Chrysler is recalling certain 2022 Jeep Gladiator vehicles due to a defective transmission park pawl that may not properly engage, potentially causing vehicle rollaway.
Pizza John's is recalling approximately 156,498 pounds of frozen pepperoni pizzas produced without federal inspection. The products were distributed in Maryland.
Epoch Everlasting Play is recalling about 8,200 Kidoozie My First Activity Desk Toys due to entanglement and entrapment hazards. A protruding knob can become entangled with clothing, and the handle opening poses a jaw entrapment risk to children under 18 months.
Rivian is recalling certain 2022 R1T and R1S vehicles because front seat belt anchors may be inadequately attached to the B-pillar, potentially preventing proper restraint during a crash.
Navitas steel rolling chassis for utility vehicles are recalled because the throttle pedal can stick in the depressed position, creating crash and injury hazards. About 3,700 units distributed nationwide from June 2020 through April 2022 are affected.
Certain 2021 Jeep Gladiator vehicles have a radio software error that may prevent the rearview camera image from displaying. This reduces rear visibility and increases the risk of backing collisions.
About 190 Big Game Hunters Mud Kitchens are being recalled because the brass water tap contains lead levels that exceed federal safety limits. Lead is toxic if ingested by young children.
Huffy Corporation is recalling about 28,550 Blue's Clues Foot to Floor Ride-on Toys because the toy can tip forward when young children ride it, causing falls and injuries. The company has received 19 reports of children falling forward, resulting in 18 facial injuries.
Trek is recalling Model Year 2022 Speed Concept SLR bicycles, MY 2021-2022 Emonda SLR bicycles, and MY 2020-2021-2022 Bontrager Aeolus RSL VR-C aftermarket handlebar stems because carbon handlebars can crack, posing fall and crash hazards.
IKEA is recalling METALLISK Espresso Makers with stainless-steel safety valves because the units can burst and expel hot contents, causing burn and scald injuries. About 2,100 units sold in the U.S. are affected.
Polaris Industries is recalling about 2,300 Model Year 2022 PATRIOT BOOST RMK KHAOS and PATRIOT BOOST PRO RMK snowmobiles because the primary clutch bolt can break, causing clutch components to separate and create a projectile hazard.
Medek LLC is recalling M Hand Sanitizer due to FDA analysis finding methanol contamination and ethanol levels below label claims. Approximately 256 bottles distributed in Texas.
Kingdom Creamery of Vermont is recalling 8.5% Gelato Mix due to potential Listeria monocytogenes contamination. The recall involves 1,623 cases distributed in Vermont, Maine, and Massachusetts.
Kingdom Creamery of Vermont's 14% Base Mix is being recalled due to potential Listeria monocytogenes contamination. The product was distributed in Vermont, Maine, and Massachusetts.
New Flyer is recalling 2021-2022 transit buses because incorrectly assembled steering gears may fracture, potentially causing a loss of steering control.
Philip R's Sorbet Co. Inc. sorbet products are being recalled due to potential Listeria monocytogenes contamination. Affected products were distributed in Vermont, Maine, and Massachusetts.
Wilbur's of Maine Milk Chocolate Covered Blueberries are recalled because the product contains undeclared almonds, posing a risk to consumers with almond allergies.
Kingdom Creamery of Vermont is recalling its 5% Maple Soft Serve Mix due to potential Listeria monocytogenes contamination. The affected product was distributed in Vermont, Maine, and Massachusetts.
Kingdom Creamery of Vermont is recalling 14% Base Mix and Archie Case Mix ice cream base products due to Listeria monocytogenes contamination. A Class I FDA recall affects 1,623 cases distributed to Vermont, Maine, and Massachusetts.
Kingdom Creamery of Vermont LLC is recalling Rococo Ice Cream 15% base mix due to potential Listeria monocytogenes contamination. The recalled product was distributed in Vermont, Maine, and Massachusetts.
Kingdom Creamery of Vermont is recalling 10% Vanilla Soft Serve Mix in specific lots due to potential Listeria monocytogenes contamination. The affected product was distributed in Vermont, Maine, and Massachusetts.
Kingdom Creamery of Vermont LLC is recalling Lake Champlain Chocolates 14% base mix due to potential Listeria monocytogenes contamination. The product was distributed in Vermont, Maine, and Massachusetts.
SOCO Creamery ice cream base mix is being recalled due to potential Listeria monocytogenes contamination. Affected consumers in Vermont, Maine, and Massachusetts should discard the product.
Kingdom Creamery of Vermont soft serve mix is recalled for possible Listeria contamination. Affected products were distributed in Vermont, Maine, and Massachusetts.
Wismettac Asian Foods recalls Marutomo Dashi Soup Base due to undeclared wheat and soy allergens. The product may pose serious allergic reaction risk to sensitive consumers.
Albertsons ready-to-eat meals may contain undeclared fish, shellfish, egg, wheat, and soy allergens. Consumers with allergies should not consume and should return the product.
Albertsons Companies LLC is recalling Ready Meals Snow Crab Legs Imitation Surimi (UPC 23463900000) for undeclared fish, shellfish, egg, and wheat allergens. Affected products have sell-through dates up to July 18.
Albertsons Companies recalled Ready Meals Shrimp Cooked with Cocktail Sauce for undeclared fish and shellfish allergens. The product was distributed across 24 US states.
Kingdom Creamery of Vermont 10% Chocolate Soft Serve Mix is being recalled due to potential Listeria monocytogenes contamination. The product was distributed in Vermont, Maine, and Massachusetts.
Kingdom Creamery of Vermont is recalling 1,623 cases of 14% Chocolate Base Mix (Lot 220724, Best By Date 8/11/22) distributed in VT, ME, and MA due to potential Listeria monocytogenes contamination.
Kingdom Creamery of Vermont is recalling 5% Vanilla Soft Serve Mix due to potential Listeria monocytogenes contamination. The affected product was distributed in Vermont, Maine, and Massachusetts.
Kingdom Creamery of Vermont's 10% Maple Soft Serve Mix is being recalled due to potential Listeria monocytogenes contamination. The affected product was distributed in Vermont, Maine, and Massachusetts.
HeartWare HVAD System Batteries are being recalled due to electrical faults that may prevent the battery from powering the device controller, accepting charges, or maintaining charge. Approximately 19,616 batteries distributed worldwide are affected.
Family Dollar is recalling Fixodent Org Cream denture adhesive (2.4oz and 0.75oz travel sizes) sold May-June 2022 due to improper storage in non-temperature-controlled areas. No illnesses reported.
Aire-Master of America Inc is recalling Common Sense Fragrance Free Hand Sanitizer due to a manufacturing process deviation. The product was made using deionized water from a system that lacked appropriate microbial control.
Nephron Sterile Compounding Center is recalling 2,030 bags of injectable bupivacaine due to potential cross-contamination from manufacturing process defects. No illnesses have been reported.
Factor is recalling 849 units of Sweet Pea Risotto & Roasted Brussel Sprouts due to glass fragments in the arborio rice ingredient. No illnesses have been reported.
Zydus Pharmaceuticals recalls Fulvestrant Injection lot B200076 due to failed purity and stability specifications. Distributed nationwide; expiration January 31, 2024.
Nephron Sterile Compounding Center is recalling one lot of Neostigmine Methylsulfate Injection due to potential cross-contamination from product carryover during manufacturing. The recall affects 13,500 vials distributed nationwide.
Nephron Sterile Compounding Center is recalling PF-Labetalol HCl Injection nationwide due to manufacturing deviations that create potential for cross-contamination. No illnesses have been reported.
Akorn, Inc. is recalling 14,712 bottles of PrednisoLONE Oral Solution (15 mg/5 mL) due to incomplete induction seals in containers. No illnesses have been reported, but the defect may affect product integrity.
Protect U Guard Foaming Hand Sanitizer is being recalled because it was manufactured with deionized water from a system lacking proper microbial controls. The affected product was distributed in Florida, Illinois, Iowa, and New Jersey.
Nephron Sterile Compounding Center is recalling 294 bags of Trisodium Citrate 0.5% Solution IV bags due to potential cross-contamination from manufacturing deviations. The affected lots were distributed nationwide.
Aire-Master of America is recalling Avant Foaming Hand Sanitizer due to a manufacturing process deviation where the deionized water system lacked proper microbial controls during production.
Baxter Healthcare recalls 85,680 bags of acetaminophen injection nationwide due to temperature abuse in distribution. Product was shipped in refrigerated trucks despite being labeled for room temperature storage.
Aire-Master of America Inc. is recalling Avant Foaming Hand Sanitizer because the deionized water system used in manufacturing lacked appropriate microbial control measures.
Micro Therapeutics is recalling Echelon-14 microcatheters whose outer carton packaging was exposed to a wet substance during transport, posing a risk to device sterility.
Clearblue Smart Countdown pregnancy tests distributed to Family Dollar stores were not stored in temperature-controlled conditions. Consumers who purchased this product should return it for a refund or replacement.
Family Dollar is recalling CURAD First Aid Kits (SKU 999037) that were improperly stored without temperature control from April 30 to June 10, 2022. The temperature exposure may have degraded medications or compromised medical devices within the kits.
Becton Dickinson recalls 9,340 units of BD PhaSeal Y-Site Connectors (Catalog 515304) due to incorrect expiration dates printed on product labels that extend beyond the actual product expiration.
Factor is recalling its Caramelized Onion & Goat Cheese Risotto due to glass fragments in an arborio rice ingredient. The contamination poses a choking and injury risk.
Factor Shrimp & Asparagus Risotto with pesto green beans is being recalled because the arborio rice ingredient contains glass. Consumers should not consume this product.
Luminex Corporation recalled 257 units of the ARIES SARS-CoV-2 Assay (lot AB4042A) due to potential false negative results. The assay may fail to detect the ORF1ab gene, risking missed COVID-19 infections.
Family Dollar is recalling LIFESTYLES ULTRA SENSITIVE CONDOMS 12CT that were stored without proper temperature control. Customers should discontinue use of product purchased between May 1 and June 10, 2022.
Trinity Sterile's Wolf Pak Premium Dressing Change Kit is mislabeled as latex-free but contains natural rubber latex in component 94-7002. This poses a risk to people with latex allergies.
Micro Therapeutics is recalling Echelon-14 Micro Catheters because outer packaging was exposed to moisture during transport. The moisture exposure could compromise the sterility or function of the device.
Family Dollar is recalling Veriquick Pregnancy Test 2CT kits (SKU 903756) sold from May 1 to June 10, 2022 due to improper storage outside temperature-controlled areas.
Family Dollar is recalling BIOTRU Multi-Purpose Solution (4 oz, SKU 999009) due to improper temperature-controlled storage. Approximately 1,051 units were affected across US Family Dollar stores.
Stradis Medical recalls 850 surgical forceps (NARMD MEDICAL DEPOT Forceps, part ZZ-0701) due to potentially compromised sterile barriers. Healthcare facilities with these units should identify affected lot numbers and contact the manufacturer for guidance.
Wolf-Pak Premium Dressing Kits labeled latex-free are being recalled because a component contains natural rubber latex, posing a risk to people with latex allergies.
Abbott Molecular is recalling the Alinity m System due to incorrect optical calibration. The affected unit (Serial Number 00654) was distributed to Italy.
Nephron Pharmaceuticals is recalling Ketorolac Tromethamine Injection due to manufacturing deviations that could lead to cross-contamination. The recall affects 5,040 vials distributed nationwide.
Crown Prince Quality Smoked Baby Clams (3 oz cans, UPC 0 73230 00853 5) are recalled due to detectable PFAS contamination. Approximately 211,716 cans distributed nationwide are affected.
USDA FSIS issued a public health alert for poultry and meat products containing corn starch with undeclared milk. Consumers should not eat these products.
Trinity Sterile's IV catheter dressing trays are mislabeled as latex-free despite containing natural rubber latex in component 94-7002, risking allergic reactions in latex-sensitive users.
Trinity Sterile is recalling Wolf Pak Premium Dressing Change Kits labeled as latex-free. The Non-Adherent Dressing component contains natural rubber latex, creating risk for patients with latex allergies.
Stradis Medical is recalling NARMD MEDICAL DEPOT Kelly Straight forceps because the sterile barrier may be compromised. The recall affects 825 units distributed nationwide in South Carolina.
GS Saline Solution (12 fl oz) was not stored in temperature-controlled areas, risking contamination. The affected product was sold at Family Dollar stores nationwide from May 1–June 10, 2022.
Myolyn Inc. is recalling the power electronic box subassembly for the MyoCycle MC-2 because internal mounting screws may come loose during shipping, creating a risk of electrical shock.
Simply Saline Nasal Mist 3.1 oz sold at Family Dollar stores has been recalled due to improper temperature storage between May and June 2022. Consumers should return the product to their local Family Dollar store.
ASO LLC is recalling 274,458 retail packages of three wound care products that fall apart during handling after removal from packaging, compromising their sterility and usability.
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